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"Nanotek" Influenza A and B Rapid Fluorescence Immunoassay Assay Kit (Unsterilized) - Taiwan Registration 87fae6cfc2fec23779d9839eef826ea9

Access comprehensive regulatory information for "Nanotek" Influenza A and B Rapid Fluorescence Immunoassay Assay Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87fae6cfc2fec23779d9839eef826ea9 and manufactured by Nano-Ditech Corporation. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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87fae6cfc2fec23779d9839eef826ea9
Registration Details
Taiwan FDA Registration: 87fae6cfc2fec23779d9839eef826ea9
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Device Details

"Nanotek" Influenza A and B Rapid Fluorescence Immunoassay Assay Kit (Unsterilized)
TW: โ€œๅฅˆ็ฑณ้ตๅ…‹โ€ ๆตๆ„Ÿ็—…ๆฏ’Aๅž‹ๅ’ŒBๅž‹ๅฟซ้€Ÿ่žขๅ…‰ๅ…็–ซๅˆ†ๆžๆชขๆธฌๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

87fae6cfc2fec23779d9839eef826ea9

DHA09402023400

Company Information

United States

Product Details

It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the "Microbial Sample Collection and Transportation Equipment (C.2900)" of the Measures for the Classification and Grading of Medical Devices.

C Immunology and microbiology

C.2900 Apparatus for collecting and delivering microbiological samples; C.3330 Influenza virus serum test

import

Dates and Status

Mar 25, 2019

Mar 25, 2024